SCHEMBL155132

SCHEMBL155132

CCOc1cc2cc(CO)c(CO)c(-c3ccn(CCOC)c(=O)c3)c2cc1OCC

nearest known ligand 0.70

Predicted protein targets (top 13)

geneUniProtsupporting neighboursconfidence
PDE4A P27815 20/20 0.70
PDE4B Q07343 20/20 0.70
PDE4C Q08493 20/20 0.70
PDE4D Q08499 20/20 0.70
PDE3B Q13370 20/20 0.70
PDE3A Q14432 20/20 0.70
PDE5A O76074 19/20 0.70
PDE1A P54750 14/20 0.50
PDE1B Q01064 14/20 0.50
PDE1C Q14123 14/20 0.50
PDE2A O00408 2/20 0.46
PDE7A Q13946 1/20 0.46
PDE7B Q9NP56 1/20 0.46

Click a target to see other patent compounds predicted against it — the reverse direction, in place.

Similar compounds — the chemically nearest patent molecules

Nearest neighbours by Morgan-fingerprint cosine across the patent-compound collection, with each neighbour's top predicted target and the predicted targets it shares with this molecule.

Compoundsimilaritytop predictedshared targets
SCHEMBL29623702 1.00 PDE4A (0.70) PDE4APDE4BPDE4CPDE4DPDE3B
SCHEMBL7285109 0.97 PDE4A (0.75) PDE4APDE4BPDE4CPDE4DPDE3B
SCHEMBL2473235 0.91 PDE4A (0.71) PDE4APDE4BPDE4CPDE4DPDE3B
SCHEMBL15085278 0.90 PDE5A (0.57) PDE4APDE4BPDE4CPDE4DPDE3B
SCHEMBL7289581 0.86 PDE4A (0.60) PDE4APDE4BPDE4CPDE4DPDE3B
SCHEMBL15085332 0.86 PDE4A (0.53) PDE4APDE4BPDE4CPDE4DPDE3B
SCHEMBL12013957 0.83 PDE4A (0.60) PDE4APDE4BPDE4CPDE4DPDE3B
SCHEMBL7287261 0.82 PDE4A (1.00) PDE4APDE4BPDE4CPDE4DPDE3B
SCHEMBL7285598 0.79 PDE4A (0.76) PDE4APDE4BPDE4CPDE4DPDE3B
SCHEMBL7279127 0.77 PDE4A (0.74) PDE4APDE4BPDE4CPDE4DPDE3B

Similarity is cosine over the 2,048-bit Morgan fingerprint (≈ Tanimoto). Identical fingerprints score 1.00.

Patent provenance — the patents this molecule appears in, and who filed them

Claimed or disclosed in 493 patents — showing the first 20. claimed = in the patent's claims; disclosed = body only.

PatentTitleAssigneePublishedPriorityFilingCountryStatus
EP-2828242-B1 NOVEL POLYMORPHIC CRYSTAL FORMS OF 5-(2-{[6-(2,2-DIFLUORO-2-PHENYLETHOXY)HEXYL]AMINO}-1-(R)-HYDROXYETHYL)-8-HYDROXYQUINOLIN-2(1H)-ONE, HEMINAPADISYLATE AS AGONIST OF THE ß2 ADRENERGIC RECEPTOR. ALMIRALL SA (ES) 2017-10-04 EP claimed
US-9346759-B2 Polymorphic crystal forms of 5-(2-{[6-(2,2-difluoro-2-phenylethoxy)hexyl]amino}-1-(R)-hydroxyethyl)-8-hydroxyquinolin-2(1H)-one, heminapadisytlate as agonist of the β2 adrenergic receptor ALMIRALL, S.A. (ES) 2016-05-24 US claimed
US-20150057256-A1 NOVEL POLYMORPHIC CRYSTAL FORMS OF 5-(2--1-(R)-HYDROXYETHYL)-8-HYDROXYQUINOLIN-2(1H)-ONE, HEMINAPADISYTLATE AS AGONIST OF THE BETA2 ADRENERGIC RECEPTOR ALMIRALL S.A. (ES) 2015-02-26 US claimed
EP-2641900-A1 Novel polymorphic Crystal forms of 5-(2-{[6-(2,2-difluoro-2-phenylethoxy) hexyl]amino}-1-(R)-hydroxyethyl)-8-hydroxyquinolin-2(1h)-one, heminapadisylate as agonist of the ß2 adrenergic receptor. Almirall, S.A. (ES) 2013-09-25 EP claimed
EP-2121615-B1 NAPADISYLATE SALT OF 5-(2-{[6-(2,2-DIFLUORO-2-PHENYLETHOXY)HEXYL]AMINO}-1-HYDROXYETHYL)-8-HYDROXYQUINOLIN-2(1H)-ONE AS AGONIST OF THE BETA 2 ADRENERGIC RECEPTOR ALMIRALL SA (ES) 2012-03-28 EP claimed
US-20110195943-A9 NAPADISYLATE SALT OF 5-(2--1-HYDROXYETHYL)-8-HYDROXYQUINOLIN-2(1H)-ONE AS AGONIST OF THE BETA 2 ADRENERGIC RECEPTOR ALMIRALL, S.A. (ES) 2011-08-11 US claimed
US-20100093681-A1 NAPADISYLATE SALT OF 5-(2--1-HYDROXYETHYL)-8-HYDROXYQUINOLIN-2(1H)-ONE AS AGONIST OF THE BETA 2 ADRENERGIC RECEPTOR ALMIRALL, S.A. (ES) 2010-04-15 US claimed
US-7659273-B2 adminstering phosphodiesterase-4 inhibitor selected from 2,3-bis(hydroxymethyl)-6,7-diethoxy-1-[1-(2-methoxyethyl)-2-oxo-4-pyridyl]naphthalene or 2,3-bis(hydroxymethyl) -6,7-diethoxy-1-[2-(4-(3-pyridyl)-1(2H)-phthaladinon-2-yl)-4-pyridyl]naphthalene MITSUBISHI TANABE PHARMA CORPORATION (JP) 2010-02-09 US claimed
US-20080031958-A1 adminstering phosphodiesterase-4 inhibitor selected from 2,3-bis(hydroxymethyl)-6,7-diethoxy-1-[1-(2-methoxyethyl)-2-oxo-4-pyridyl]naphthalene or 2,3-bis(hydroxymethyl) -6,7-diethoxy-1-[2-(4-(3-pyridyl)-1(2H)-phthaladinon-2-yl)-4-pyridyl]naphthalene TANABE SEIYAKU CO., LTD. 2008-02-07 US claimed
US-20070155652-A1 Composition for regenerative treatment of cartilage disease TANABE SEIYAKU CO., LTD. 2007-07-05 US claimed
US-20040180900-A1 Therapeutic composition for repairing chondropathy TANABE SEIYAKU CO., LTD. (JP) 2004-09-16 US claimed
US-20040146561-A1 Compositions for promoting healing of bone fracture TANABE SEIYAKU CO., LTD. (JP) 2004-07-29 US claimed
EP-1389468-A1 COMPOSITIONS FOR PROMOTING HEALING OF BONE FRACTURE TANABE SEIYAKU CO., LTD. (JP) 2004-02-18 EP claimed
EP-1389467-A1 THERAPEUTIC COMPOSITIONS FOR REPAIRING CHONDROPATHY TANABE SEIYAKU CO., LTD. (JP) 2004-02-18 EP claimed
EP-0557016-B1 Naphthalene derivatives, processes for preparing the same, and synthetic intermediates therefor TANABE SEIYAKU CO (JP) 1996-06-19 EP claimed
US-5342941-A Bronchodilating agents TANABE SEIYAKU CO., LTD. (JP) 1994-08-30 US claimed
US-20250205232-A1 MODULATORS OF CYSTIC FIBROSIS TRANSMEMBRANE CONDUCTANCE REGULATOR VERTEX PHARMACEUTICALS INCORPORATED (US) 2025-06-26 US disclosed
US-20250115561-A1 BIPHENYL-SUBSTITUTED EPITHELIAL SODIUM CHANNEL BLOCKING COMPOUNDS PARION SCIENCES, INC. (US) 2025-04-10 US disclosed
US-5342941-A Bronchodilating agents TANABE SEIYAKU CO., LTD. (JP) 1994-08-30 US disclosed
EP-0557016-A1 Naphthalene derivatives, processes for preparing the same, and synthetic intermediates therefor TANABE SEIYAKU CO., LTD. (JP) 1993-08-25 EP disclosed

Patent text — is the patent's own abstract consistent with the prediction?

For each of this compound's patents that has machine-readable text (9 of them — usually the abstract, not the full specification), we ask MedCPT which protein the text reads most about, and where the chemistry-predicted target lands among 4885 human targets. A high rank means the patent's own wording is consistent with the prediction — a weak, independent signal, not proof of activity.

PatentTitleText reads most aboutPredicted target · text-rank
US-20250115561-A1 BIPHENYL-SUBSTITUTED EPITHELIAL SODIUM CHANNEL BLOCKING COMPOUNDS CFTR, SCNN1B, SCNN1G PDE4A 455/4885PDE4B 330/4885PDE4C 534/4885
US-20080031958-A1 adminstering phosphodiesterase-4 inhibitor selected from 2,3-bis(hydroxymethyl)-6,7-diethoxy-1-[1-(2-methoxyethyl)-2-oxo-4-pyridyl]naphthalene or 2,3-bis(hydroxymethyl) -6,7-diethoxy-1-[2-(4-(3-pyridyl)-1(2H)-phthaladinon-2-yl)-4-pyridyl]naphthalene PDE4A, PDE7A, PDE4B PDE4A 1/4885PDE4B 3/4885PDE4C 7/4885
US-20250205232-A1 MODULATORS OF CYSTIC FIBROSIS TRANSMEMBRANE CONDUCTANCE REGULATOR CFTR, SCNN1B, SLC26A4 PDE4A 357/4885PDE4B 399/4885PDE4C 506/4885
US-20040180900-A1 Therapeutic composition for repairing chondropathy PDE4B, PDE4A, PDE4C PDE4A 2/4885PDE4B 1/4885PDE4C 3/4885
US-20150057256-A1 NOVEL POLYMORPHIC CRYSTAL FORMS OF 5-(2--1-(R)-HYDROXYETHYL)-8-HYDROXYQUINOLIN-2(1H)-ONE, HEMINAPADISYTLATE AS AGONIST OF THE BETA2 ADRENERGIC RECEPTOR ADRA2C, ADRB2, ADRA2A PDE4A 367/4885PDE4B 274/4885PDE4C 462/4885
US-20100093681-A1 NAPADISYLATE SALT OF 5-(2--1-HYDROXYETHYL)-8-HYDROXYQUINOLIN-2(1H)-ONE AS AGONIST OF THE BETA 2 ADRENERGIC RECEPTOR ADRA2C, ADRB2, ADRA2A PDE4A 261/4885PDE4B 237/4885PDE4C 361/4885
US-20040146561-A1 Compositions for promoting healing of bone fracture PDE4B, PDE4A, PDE4D PDE4A 2/4885PDE4B 1/4885PDE4C 4/4885
US-20070155652-A1 Composition for regenerative treatment of cartilage disease PDE4B, PDE4A, PDE4C PDE4A 2/4885PDE4B 1/4885PDE4C 3/4885
US-20110195943-A9 NAPADISYLATE SALT OF 5-(2--1-HYDROXYETHYL)-8-HYDROXYQUINOLIN-2(1H)-ONE AS AGONIST OF THE BETA 2 ADRENERGIC RECEPTOR ADRA2C, ADRB2, ADRA2A PDE4A 261/4885PDE4B 237/4885PDE4C 361/4885

“Text reads most about” is the patent abstract's nearest protein in MedCPT space (background-debiased). Only ~1.4% of patents have machine-readable text, so most compounds won't have this panel.